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rs5030777

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs5030777(C;C)
Make rs5030777(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position30233708
GeneFSHB, LOC105376607
is asnp
is mentioned by
dbSNPrs5030777
ebirs5030777
HLIrs5030777
Exacrs5030777
Varsomers5030777
Maprs5030777
PheGenIrs5030777
hapmaprs5030777
1000 genomesrs5030777
hgdprs5030777
ensemblrs5030777
gopubmedrs5030777
geneviewrs5030777
scholarrs5030777
googlers5030777
pharmgkbrs5030777
gwascentralrs5030777
openSNPrs5030777
23andMers5030777
23andMe allrs5030777
SNP Nexus

SNPshotrs5030777
SNPdbers5030777
MSV3drs5030777
GWAS Ctlgrs5030777
Max Magnitude0
ClinVar
Risk rs5030777(C;C)
Alt rs5030777(C;C)
Reference rs5030777(T;T)
Significance Pathogenic
Disease Follicle-stimulating hormone deficiency
Variation info
Gene FSHB
CLNDBN Follicle-stimulating hormone deficiency, isolated
Reversed 0
HGVS NC_000011.9:g.30255255T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000169745.4,